Search Results - "Modell B"

Hemoglobinopathy Prevention Program in Immigrants: Equality Plus Education Program.

Authors: Canatan, Duran De Sanctis, Vincenzo Vives Corrons, Joan Lluis et al.

Source: Thalassemia Reports. Mar2026, Vol. 16 Issue 1, p4. 6p.

Disease Burden in Transfusion-Dependent β-Thalassemia (TDT) Patients and Caregivers in Italy: Results of a Cross-Sectional Descriptive Online Survey.

Authors: Contieri M Gatta F Colonnese M et al.

Source: Drugs - real world outcomes [Drugs Real World Outcomes] 2026 Jun; Vol. 13 (2), pp. 289-298. Date of Electronic Publication: 2026 Mar 27.

Publication Type: Journal Article

Journal Info: Publisher: Springer International Publishing Country of Publication: Switzerland NLM ID: 101658456 Publication Model: Print-Electronic Cited Medium: Print ISSN: 2199-1154 (Print) Linking ISSN: 21989788 NLM ISO Abbreviation: Drugs Real World Outcomes Subsets: PubMed not MEDLINE

Birth Defect Clinic – An Integrated Approach to the Management of 1549 Antenatally Diagnosed Anomalies in a Tertiary Care Center.

Authors: Parelkar, Sandesh Vinod Makhija, Deepa Prashant Sanghvi, Beejal et al.

Source: Journal of Indian Association of Pediatric Surgeons. Jan/Feb2026, Vol. 31 Issue 1, p73-76. 4p.

Folic acid supplementation during preconception period in sub-Saharan African countries: A systematic review and meta-analysis.

Authors: Aweke, Mekuriaw Nibret Fentie, Elsa Awoke Agimas, Muluken Chanie et al.

Source: PLoS ONE. 1/31/2025, Vol. 20 Issue 1, p1-24. 24p.

Investigation of osteoprotegerin gene polymorphisms and serum level as a predictive marker of cardiac abnormalities in beta thalassemia major.

Authors: Pourrahim, Elham Badiei, Zahra shahri, Hassan Mottaghi moghaddam et al.

Source: Egyptian Journal of Medical Human Genetics. 6/11/2026, Vol. 27 Issue 1, p1-8. 8p.

Large population-based assessment of SARS-CoV-2 teratogenicity by profiling congenital anomalies during COVID-19 pandemic.

Authors: Jehangir, Susan Navaneethan, Preethi R. Karuppasami, Reka et al.

Source: Journal of the Turkish-German Gynecological Association. Jun2026, Vol. 27 Issue 2, p1-8. 8p.

Challenges and opportunities in hydroxyurea access and adherence for sickle cell disease patients at Komfo Anokye Teaching Hospital: Insights from healthcare providers.

Authors: Mensah, Josephine Marfo, Afia Frimpomaa Asare Opare-Addo, Mercy Naa Aduele et al.

Source: PLoS ONE. 5/29/2026, Vol. 21 Issue 5, p1-14. 14p.

The hyperdynamic paradox: 3D speckle-tracking unmasks subclinical RV dysfunction in pediatric transfusion-dependent beta-thalassemia.

Authors: Raafat, Omar Aboukhalil, Mohamed Ahmed Chazli, Yasmine El et al.

Source: Egyptian Pediatric Association Gazette. 5/22/2026, Vol. 74 Issue 1, p1-9. 9p.

Application of Management, Outcome, Risk, and Expectation Classification for Antenatally Suspected Structural Anomalies: A Multidisciplinary Experience.

Authors: Singh, Sunita Prakash, Divya Borkar, Nitin Kumar et al.

Source: Journal of Indian Association of Pediatric Surgeons. May/Jun2026, Vol. 31 Issue 3, p427-435. 9p.

Micronutrient Intake, Supplementation Practices and Lifestyle Among Pregnant Women in Greece: A Review.

Authors: Kapellou, Angeliki Koutelidakis, Antonios E. Stoupi, Stavroula

Source: Applied Sciences (2076-3417); Jan2026, Vol. 16 Issue 1, p429, 19p

Reproductive functions and fertility preservation in men with sickle cell disease.

Authors: Leblanc, Clarisse Sermondade, Nathalie Rivet‐Danon, Diane et al.

Source: Andrology. Nov2025, Vol. 13 Issue 8, p2142-2149. 8p.

Congenital malformations-related mortality trends in under-five U.S. children: A 24-year analysis from CDC-WONDER database (1999–2023).

Authors: Rath, Shree Hasan, Ahmed Ali, Muhammad et al.

Source: Journal of Neonatal - Perinatal Medicine. Sep2026, Vol. 19 Issue 5, p484-494. 11p.

کمخونی یک مسئله در سالمت جهانی.

Alternate Title: Anemia as a Global Health Issue.

Authors: سیده زهره جاللی¹ z_jalali@gums.ac.ir

Source: Journal of Guilan University of Medical Sciences. Spring2026, Vol. 35 Issue 1, p2-7. 5p.

Transition from Pediatric to Adult Care in Patients with Transfusion-Dependent Beta-Thalassemia in France: A National Study Concerning a Rare Disease.

Authors: Szepetowski, Sarah Benoit, Audrey Berbis, Julie et al.

Source: Journal of Clinical Medicine. Mar2026, Vol. 15 Issue 6, p2203. 13p.

Healthcare providers' knowledge on sickle cell disease and its management: A pre- and post-training test evaluation outcome.

Authors: Paintsil, Vivian Amuzu, Evans Xorse Ahmed, Eunice et al.

Source: PLoS ONE. 9/8/2025, Vol. 20 Issue 9, p1-11. 11p.

Nephrological Complications in Hemoglobinopathies: SITE Good Practice.

Authors: Ruffo, Giovan Battista Russo, Rodolfo Casini, Tommaso et al.

Source: Journal of Clinical Medicine. Dec2023, Vol. 12 Issue 23, p7476. 8p.

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The Heterogeneous Global Burden of Hemoglobinopathies Among Women of Childbearing Age, 1990-2021, with Projection to 2030.

Authors: Wu, Huiqiang Cai, Zhiyin Liu, Wanyi et al.

Source: International Journal of Women's Health. Jan2026, Vol. 18, p1-18. 18p.

A systematic review of the prevalence and phenotypic characteristics of hemoglobin Malay in Southeast Asia.

Authors: Zulkeflee, Razan Hayati Ramli, Marini Halim, Sarah Abdul et al.

Source: Iraqi Journal of Hematology. Jan-Jun2026, Vol. 15 Issue 1, p8-15. 8p.

A blueprint for fortification planning and programming: Lessons learned from an analytical review of existing fortification frameworks.

Authors: Darwar, Roopa Rowe, Laura A. Chadha, Manpreet et al.

Source: Maternal & Child Nutrition. Jan2026, Vol. 22 Issue 1, p1-13. 13p.